Cholesterol Synthesis and Skeletal Formation
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Reference4 articles.
1. Mutations in the gene encoding 3β- hydroxysteroid-Δ8,Δ7- isomerase cause X-linked dominant Conradi-Hünermann syndrome
2. Mutations in a Δ8-Δ7 sterol isomerase in the tattered mouse and X-linked dominant chondrodysplasia punctata
3. Abnormal sterol metabolism in patients with Conradi-H�nermann-Happle syndrome and sporadic lethal chondrodysplasia punctata
4. The gene mutated in bare patches and striated mice encodes a novel 3β-hydroxysteroid dehydrogenase
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1. Progressive Early-onset Scoliosis in Conradi Disease;Journal of Pediatric Orthopaedics;2013-03
2. Specific entities affecting the craniocervical region: syndromes affecting the craniocervical junction;Child's Nervous System;2008-03-28
3. Cervical spine stenosis in chondrodysplasia punctata;Journal of Pediatric Orthopaedics B;2007-11
4. Spinal Deformity in Chondrodysplasia Punctata;Spine;2002-09
5. Stability of Filgrastim and Epoetin Alfa in a System Designed for Enteral Administration in Neonates;Annals of Pharmacotherapy;2000-11
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